期刊
JOURNAL OF PHARMACEUTICAL SCIENCES
卷 111, 期 11, 页码 3108-3113出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.xphs.2022.07.010
关键词
Chemical stability; Solid-state stability; Degradation product; Kinetics; Mathematical model; Tablet; Formulation
By establishing statistical and kinetic models, as well as precise parameter estimates, the study successfully investigated the chemical degradation mechanism of candesartan cilexetil under pressure conditions and developed a stable formulation. The results of this study facilitate timely evaluation of future product changes.
Candesartan cilexetil is challenging to formulate due to pressure induced chemical degradation. We report a statistical model based on stability data set of a marketed tablet formulation. Impurity increase over time was fitted to a reparametrized second-order kinetic model. Both kinetic model parameters have mechanistic interpretation: parameter a relates to the overall extent of pressure induced instability (the ceiling impurity level) and parameter b relates to the initial rate of degradation (how fast the ceiling is reached). A hierarchi-cal model was then used to quantify sensitivity to tableting pressure and humidity-corrected Arrhenius equation quantified sensitivity to temperature and moisture. An overall model, based on four predictors and five estimated parameters allowed fitting of the entire stability dataset (694 stability data points) with good accuracy. Learnings allowed development of a stable formulation (soft tableting, increasing tablet size/shape and reducing moisture) and resulted in a confident stress stability test to evaluate any future product changes in a timely manner.(c) 2022 American Pharmacists Association. Published by Elsevier Inc. All rights reserved.
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